Evaluation of phytotoxic potential and identification of phytotoxic compounds in Rumex maritimus

References

• Ahmed M, Datta BK, Rouf ASS. 1991. Anthraquinone, chromone and flavone derivatives from Rumex maritimus. Pharmazie 46: 548–549.
   Web of Science ®Google Scholar
• Alfawaz MA. 2006. Chemical composition of hummayd (Rumex vesicarius) grown in Saudi Arabia. J Food Compos Anal 19: 552–555.10.1016/j.jfca.2004.09.004
   Web of Science ®Google Scholar
• Andersen B, Nielsen KF, Fernández Pinto V, Patriarca A. 2015. Characterization of Alternaria strains from Argentinean blueberry, tomato, walnut and wheat. Int J Food Microbiol 196: 1–10.10.1016/j.ijfoodmicro.2014.11.029
   PubMed Web of Science ®Google Scholar
• Basile A, Cobianchi RC, Rigano D, Senatore F, Bruno M, Rosselli S, Conte B, Sorbo S. 2011. Potential allelopathic activity of Sideritis italica (Miller) Greuter et Burdet essential oil. Plant Biosyst 145: 241–247.10.1080/11263504.2010.546112
   Web of Science ®Google Scholar
• Boulos L, EI-Hadidi MN. 1984. The weed flora of Egypt. Cairo: American University Press.
   Google Scholar
• Chopra RN, Nayar SL, Chopra IC. 2002. Glossary of Indian medicinal plants. New Delhi: National Institute of Science Communication and Information resources.
   Google Scholar
• Craig CF, Reveal JL. 2005. Polygonaceae. In: Flora of North America Editorial Committee, editors. Flora of North America. New York: Oxford University Press; p. 216–601.
   Google Scholar
• Duke SO, Dayan FE, Romagni JG, Rimando AM. 2000. Natural products as sources of herbicides: current status and future trends. Weed Res 40: 99–111.10.1046/j.1365-3180.2000.00161.x
   Web of Science ®Google Scholar
• Fujii Y, Parvez SS, Parvez MM, Ohmae Y, Iida O. 2003. Screening of 239 medicinal plant species for allelopathic activity using the sandwich method. Weed Biol Manage 3: 233–241.10.1046/j.1444-6162.2003.00111.x
   Google Scholar
• Giday M, Asfaw Z, Woldu Z. 2009. Medicinal plants of the Meinit ethnic group of Ethiopia: An ethnobotanical study. J Ethnopharmacol 124: 513–521.10.1016/j.jep.2009.05.009
   PubMed Web of Science ®Google Scholar
• Gu W. 2009. Bioactive metabolites from Alternaria brassicicola ML-Po8, an endophytic fungus residing in Malus halliana. World J Microbiol Biotechnol 25: 1677–1683.10.1007/s11274-009-0062-y
   Web of Science ®Google Scholar
• Hussain H, Krohn K, Draeger S, Meier K, Schulz B. 2009. Bioactive chemical constituents of a sterile endophytic fungus from Meliotus dentatus. Rec Nat Prod 3: 114–117.
   Google Scholar
• Information on California plants. 2016. Information on California plants for education, research and conservation, with data contributed by public and private institutions and individuals, including the consortium of California Herbaria. [cited 2016 Dec 20]. Available from: http://www.calflora.org
   Google Scholar
• Islam MS, Rahman MT, Rouf ASS, Rahman F. 2003. Evaluation of neuropharmacological effects of Rumex maritimus Linn. (Polygonaceae) root extracts. Pharmazie 58: 738–741.
   PubMed Web of Science ®Google Scholar
• Islam AKMM, Ohno O, Suenaga K, Kato-Noguchi H. 2014. Two novel phytotoxic substances from Leucas aspera. J Plant Physiol 171: 877–883.10.1016/j.jplph.2014.03.003
   PubMed Web of Science ®Google Scholar
• Islam MS, Iwasaki A, Suenaga K, Kato-Noguchi H. 2017. Isolation and identification of two potential phytotoxic substances from the aquatic fern Marsilea crenata. J Plant Biol 60: 75–81.10.1007/s12374-016-0408-6
   Web of Science ®Google Scholar
• Kato-Noguchi H, Suzuki M, Noguchi K, Ohno O, Suenaga K, Laosinwattana C. 2016. A potent phytotoxic substance in Aglaia odorata Lour. Chem Biodivers 13: 549–554.10.1002/cbdv.201500175
   PubMed Web of Science ®Google Scholar
• Khanh TD, Cong LC, Xuan Y, Uezato Y, Deba F, Toyama T, Tawata S. 2009. Allelopathic plants: 20 hairy beggarticks (Bidens pilosa L.). Allelopathy J 24: 243–254.
   Web of Science ®Google Scholar
• Kimura Y, Mizuno T, Nakajima H, Hamasaki T. 1992. Altechromone A and B, new plant growth regulators produced by the fungus Alternaria sp. Biosci Biotechnol Biochem 56: 1664–1665.10.1271/bbb.56.1664
   PubMed Web of Science ®Google Scholar
• Kirtikar KR, Basu BD. 1980. Indian medicinal plants. Dehradun: International Book Distributors.
   Google Scholar
• Kong C, Liang W, Xu X, Hu F, Wang P, Jiang Y. 2004. Release and activity of allelochemicals from allelopathic rice seedlings. J Agric Food Chem 52: 2861–2865.10.1021/jf035467i
   PubMed Web of Science ®Google Scholar
• Königs P, Rinker B, Maus L, Nieger M, Rheinheimer J, Waldvogel SR. 2010. Structural revision and synthesis of altechromone A. J Nat Prod 73: 2064–2066.10.1021/np1005604
   PubMed Web of Science ®Google Scholar
• Kuddus MR, Ali MB, Rumi F, Aktar F, Rashid MA. 2011. Evaluation of polyphenols content and cytotoxic, membrane stabilizing and antimicrobial activities of seed of Rumex maritimus Linn. Bangladesh Pharm J 14: 67–71.
   Google Scholar
• Lee NJ, Choi JH, Koo BS, Ryu SY, Han YH, Lee SI, Lee DU. 2005. Antimutagenicity and cytotoxicity of the constituents from the aerial parts of Rumex acetosa. Biol Pharm Bull 28: 2158–2161.10.1248/bpb.28.2158
   PubMed Web of Science ®Google Scholar
• Moussa M, Ebrahim W, El-Neketi M, Mándi A, Kurtán T, Hartmann R, Lin W, Liu Z, Proksch P. 2016. Tetrahydroanthraquinone derivatives from the mangrove-derived endophytic fungus Stemphylium globuliferum. Tetrahedron Lett 57: 4074–4078.10.1016/j.tetlet.2016.07.091
   Web of Science ®Google Scholar
• Pardo-de-Santayana M, Tardío J, Morales R. 2005. The gathering and consumption of wild edible plants in the Campoo (Cantabria, Spain). Int J Food Sci Nutr 56: 529–542.10.1080/09637480500490731
   PubMed Web of Science ®Google Scholar
• Qin B, Perry LG, Broeckling CD, Du J, Stermitz FR, Paschke MW, Vivanco JM. 2006. Phytotoxic allelochemicals from roots and root exudates of leafy spurge (Euphorbia esula L.). Plant Signal Behav 6: 323–327.10.4161/psb.1.6.3563
   Google Scholar
• Ren ZY, Qi HY, Shi YP. 2008. Phytochemical investigation of Anaphalis lacteal. Planta Med 74: 859–863.10.1055/s-2008-1074547
   PubMed Web of Science ®Google Scholar
• Rouf ASS, Islam MS, Rahman MT. 2003. Evaluation of antidiarrhoeal activity Rumex maritimus root. J Ethnopharmacol 84: 307–310.10.1016/S0378-8741(02)00326-4
   PubMed Web of Science ®Google Scholar
• Rukachaisirikul V, Rodglin A, Sukpondma Y, Phongpaichit S, Buatong J, Sakayaroj J. 2012. Phthalide and isocoumarin derivatives produced by an Acremonium sp. isolated from a mangrove Rhizophora apiculate. J Nat Prod 75: 853–858.10.1021/np200885e
   PubMed Web of Science ®Google Scholar
• Saleh NAM, El-Hadidi MN, Arafa RFM. 1993. Flavonoids and anthraquinones of some Egyptian Rumex species (Polygonaceae). Biochem Syst Ecol 21: 301–303.10.1016/0305-1978(93)90049-W
   Web of Science ®Google Scholar
• Shao P, Zhang X, Li B, Jiao WH, Wu LJ, Yao XS. 2010. New isocourmarin and phthalide derivatives from the rhizomes of Matteuccia orientalis. Chem Pharm Bull 58: 1650–1654.10.1248/cpb.58.1650
   PubMed Web of Science ®Google Scholar
• Shushni MAM, Mentel R, Lindequist U, Jansen R. 2009. Balticols A–F, new naphthalenone derivatives with antiviral activity, from an ascomycetous fungus. Chem Biodivers 6: 127–137.10.1002/cbdv.v6:2
   PubMed Web of Science ®Google Scholar
• Singh R, Jain A, Panwar S, Gupta D, Khare SK. 2005. Antimicrobial activity of some natural dyes. Dyes Pig 66: 99–102.10.1016/j.dyepig.2004.09.005
   Web of Science ®Google Scholar
• Tsai NM, Chen YL, Lee CC, Lin PC, Cheng YL, Chang WL, Lin SZ, Harm HJ. 2006. The natural compound n-butylidenephthalide derived from Angelica sinensis inhibits malignant brain tumor growth in vitro and in vivo. J Neurochem 99: 1251–1262.10.1111/jnc.2006.99.issue-4
   PubMed Web of Science ®Google Scholar
• Ullah N, Haq IU, Mirza B. 2015. Phytotoxicity evaluation and phytochemical analysis of three medicinally important plants from Pakistan. Toxicol Ind Health 5: 389–395.10.1177/0748233712472527
   Web of Science ®Google Scholar
• Vasas A, Orbán-Gyapai O, Hohmann J. 2015. The genus Rumex: review of traditional uses, phytochemistry and pharmacology. J Ethnopharmacol 175: 198–228.10.1016/j.jep.2015.09.001
   PubMed Web of Science ®Google Scholar
• Yoshikawa K, Kokudo N, Hashimoto T, Yamamoto K, Inose T, Kimura T. 2010. Novel phthalide compounds from Sparassis crispa (Hanabiratake), Hanabiratakelide A-C, exhibiting anti-cancer related activity. Biol Pharm Bull 33: 1355–1359.10.1248/bpb.33.1355
   PubMed Web of Science ®Google Scholar